Canonical Allele Identifier: CA1593395132
Gene: SGCD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.155775518A>C , CM000667.2:g.155775518A>C GRCh38
NC_000005.9:g.155202528A>C , CM000667.1:g.155202528A>C GRCh37
NC_000005.8:g.155135106A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017009724.1:c.-208+46528A>C XP_016865213.1:n.-208+46528A>C